Transcription Factor |
Target ORF/Genes |
References |
Evidence Code |
Evidence Experiment |
Association Type |
Strain |
Environmental Group |
Environmental Condition |
Log2FC |
|
Ume6p
|
YBR072W
|
PubMed
Williams RM et al., Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct 15;99(21):13431-6Williams RM et al., Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct 15;99(21):13431-6 |
Indirect |
Microarray analysis - wt vs TF mutant |
Negative |
SK1 |
Carbon source quality/availability |
Cells grown in YPAcetate medium to late log phase |
N/A |
| Indirect |
Microarray analysis - wt vs TF mutant |
Negative |
W303 |
Unstressed log-phase growth (control) |
Cells grown in YPD medium to late log phase |
N/A |
PubMed
Lardenois A et al., Molecular genetics and genomics : MGG, 2015 Oct;290(5):2031-46Lardenois A et al., Molecular genetics and genomics : MGG, 2015 Oct;290(5):2031-46 |
Indirect |
Microarray analysis - WT vs TF Deletion |
Negative |
SK1 |
Carbon source quality/availability |
Grown in rich media with acetate (YPA) under standard conditions. Transcription factor gene deletion. |
-2.339553 |
PubMed
van Heusden GPH, Genomics, 2023 Sep;115(5):110672van Heusden GPH, Genomics, 2023 Sep;115(5):110672 |
Indirect |
RNA-seq analysis - WT vs TF Deletion |
Negative |
BY4741 |
Ion/metal/phosphate/sulfur/vitamin availability |
Grown overnight at 30 °C in phosphate-free YNB medium supplemented with 7.2 mM potassium phosphate (pH 5.8), 20 mg/L histidine, leucine, methionine, and uracil, and 50 mM KCl, then used to inoculate 50 mL cultures at OD620 = 0.1 and grown at 30 °C, 180 rpm to OD620 = 0.5. Transcription factor gene deletion. |
-1.12320455089806 |
PubMed
Harris A et al., Genetics, 2023 Oct 4;225(2):Harris A et al., Genetics, 2023 Oct 4;225(2): |
Indirect |
RNA-seq analysis - WT vs TF Deletion |
Positive |
SK1 |
Unstressed log-phase growth (control) |
Mitotic, 30min: Cells were in mitotic, log-phase growth. They were grown in YPD (1% yeast extract, 2% peptone, 2% dextrose, 22.4 mg/L uracil, 80 mg/L tryptophan) for ~24 h to saturation, then back-diluted into fresh YPD to OD600 = 0.2 and grown ~3 h to log phase (OD600 ≥ 0.5). Once in log phase, β-estradiol (40 nM) was added, followed 30 min later by auxin (200 µM) at t=0min. Sampled at 30 min. |
0.741346 |
| Indirect |
RNA-seq analysis - WT vs TF Under-expression |
Negative |
SK1 |
Cell cycle/morphology |
Meiotic 0.5h: Cells were transitioning from premeiotic starvation into meiosis. They were grown in YPD for ~24 h to saturation, then inoculated into BYTA (1% yeast extract, 2% bacto tryptone, 1% potassium acetate, 50 mM potassium phthalate) at OD600 = 0.25 and grown 16–18 h at 30 °C to OD600 ≥ 5. Cells were then pelleted, washed with sterile water, and resuspended in SPM (2% KOAc, 0.02% raffinose, amino acid supplements, pH 7) at OD600 = 1.85, shaken at 30 °C and 275 rpm. At 0.5 h in SPM, β-estradiol (5 nM) and auxin (200 µM) were added simultaneously, followed by CuSO4 (50 µM) at 2 h to trigger IME1/4 expression and meiotic entry. Sampled at 0.5 h. |
-1.018074 |
| Indirect |
RNA-seq analysis - WT vs TF Under-expression |
Negative |
SK1 |
Unstressed log-phase growth (control) |
Mitotic, 15min: Cells were in mitotic, log-phase growth. They were grown in YPD (1% yeast extract, 2% peptone, 2% dextrose, 22.4 mg/L uracil, 80 mg/L tryptophan) for ~24 h to saturation, then back-diluted into fresh YPD to OD600 = 0.2 and grown ~3 h to log phase (OD600 ≥ 0.5). Once in log phase, β-estradiol (40 nM) was added, followed 30 min later by auxin (200 µM) at t=0min. Sampled at 15 min. |
-0.4033 |
| Indirect |
RNA-seq analysis - WT vs TF Under-expression |
Negative |
SK1 |
Cell cycle/morphology |
Meiotic 2.5h: Cells were transitioning from premeiotic starvation into meiosis. They were grown in YPD for ~24 h to saturation, then inoculated into BYTA (1% yeast extract, 2% bacto tryptone, 1% potassium acetate, 50 mM potassium phthalate) at OD600 = 0.25 and grown 16–18 h at 30 °C to OD600 ≥ 5. Cells were then pelleted, washed with sterile water, and resuspended in SPM (2% KOAc, 0.02% raffinose, amino acid supplements, pH 7) at OD600 = 1.85, shaken at 30 °C and 275 rpm. At 0.5 h in SPM, β-estradiol (5 nM) and auxin (200 µM) were added simultaneously, followed by CuSO4 (50 µM) at 2 h to trigger IME1/4 expression and meiotic entry. Sampled at 2.5 h. |
-1.864312 |